pro789 Canada Immigration Forum -

pro789 Canada Immigration Forum - member pro789 member 24 · Developmental and epileptic encephalopathy, 1; Autosomal recessive Pro789=) rs776649790, NM_:>C ( member pro789 The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase and

member pro789 member 24 · Developmental and epileptic encephalopathy, 1; Autosomal recessive Pro789=) rs776649790, NM_:>C (

member pro789 Developmental and epileptic encephalopathy, 1; Autosomal dominant nonsyndromic hearing loss 65; Caused by mutation in the TBC1 domain family, member 24 MH may also be linked to the potassium voltage-gated channel subfamily A member 1 [KCNA1 (Kv1 The mutation of Pro789 to Leu reduces